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Amplex™ Red Neuraminidase (Sialidase) Assay Kit
Amplex™ Red Neuraminidase (Sialidase) Assay Kit
Invitrogen™

Amplex™ Red Neuraminidase (Sialidase) Assay Kit

The Amplex™ Red Neuraminidase (Sialidase) Assay Kit provides a sensitive and simple method for detecting neuraminidase activity in serum andRead more
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Catalog NumberQuantity
A22178400 assays
Catalog number A22178
Price (USD)
-
Quantity:
400 assays
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The Amplex™ Red Neuraminidase (Sialidase) Assay Kit provides a sensitive and simple method for detecting neuraminidase activity in serum and in purified enzyme systems using either a fluorescence microplate reader or fluorometer.

See our complete line of Fluorescence Microplate assays.

• Detect neuraminidase levels as low as 0.2 mU/mL
• Format allows for multiple time point measurements
• Designed for minimal autofluorescence interference
• Detect neuraminidase activity in biological samples such as serum

Neuraminidase (also known as sialidase) is a very common enzyme that hydrolyzes terminal sialic acid residues on polysaccharide chains, most often exposing a galactose residue. Neuraminidase plays a key role in the invasion of target cells and the subsequent replication of the influenza virus, making neuraminidase an important target for influenza drug development.

The Amplex™ Red Neuraminidase (Sialidase) Assay Kit provides an ultrasensitive method for detecting neuramimidase activity. This assay utilizes Amplex™ Red reagent to detect hydrogen peroxide generated by galactose oxidase oxidation of desialiated galactose, the end result of neuraminidase action. Then the hydrogen peroxide, in the presence of horseradish peroxidase (HRP), reacts in a 1:1 stoichiometric ratio with Amplex™ Red reagent to generate the red-fluorescent oxidation product resorufin.

Because resorufin has absorption and fluorescence emission maxima of approximately 571 nm and 585 nm, respectively, there is little interference from autofluorescence in most biological samples.

Use Amplex™ Red Assays for a Broad Range of Investigations
A wide variety of validated Amplex™ Red assays are available for studying cell signaling and lipids, neurobiology, inflammation and immune function, and metabolism. We also offer Amplex™ UltraRed Reagent (Cat. No. A36006), a second-generation reagent providing greater sensitivity and brighter fluorescence, and the Amplex™ Red/UltraRed Stop Reagent (Cat. No. A33855). The Amplex™ Red/UltraRed Stop Reagent provides convenience and control by allowing the fluorescence signal-generating reaction to be terminated at a user-determined time point. After addition of the stop reagent, the fluorescence signal remains stable for at least three hours. Custom assay design and packaging are also available.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodFluorescence
Dye TypeOther Label(s) or Dye(s)
FormatTube(s), 96-well plate
Quantity400 assays
Shipping ConditionRoom Temperature
For Use With (Application)Neuraminidase (Sialidase) Assay
For Use With (Equipment)Microplate Reader, Spectrophotometer, Fluorometer
Product LineAmplex
Product TypeRed Neuraminidase (Sialidase) Assay Kit
Unit SizeEach
Contents & Storage
Store in freezer -5°C to -30°C and protect from light.
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Figures

Fluorescence spectra

Fluorescence spectra

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Lot #Certificate TypeDateCatalog Number(s)
3163194Certificate of AnalysisMay 04, 2025A22178
2770783Certificate of AnalysisNov 22, 2024A22178
2720320Certificate of AnalysisSep 27, 2023A22178
2663849Certificate of AnalysisAug 17, 2023A22178
2591125Certificate of AnalysisMar 14, 2023A22178
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Safety Data Sheets

Frequently asked questions (FAQs)

The components of Krebs-Ringer buffer (salts) should not cause oxidation of the Amplex reagent (which, in the presence of peroxidase and H2O2 oxidizes to resorufin, which is pink in color and fluorescent). Try water alone (the water used to make the Krebs-Ringer buffer). Since Hank's Buffered Saline Solution is typically purchased rather than made in the lab, it likely would not have the same contaminant. Another option is to degas the buffer prior to use to removed dissolved oxygen radicals.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

This is not recommended. The presence of endogenous proteases can complicate the assay by degrading the horseradish peroxidase (HRP). Endogenous peroxidases and antioxidants can modify the H2O2 required for the reaction, competing with HRP (and catalase) for the substrate.

The Amplex Red Assays are best performed with either purified enzymes or extracted H2O2 in a defined buffer system, extracellular solutions or body fluids (media, serum, etc.) that do not exhibit high levels of endogenous protease or oxidase activity and do not contain antioxidants.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

The assay utilizes Amplex Red to detect H2O2 generated by galactose oxidase oxidation of desialiated galactose, the result of neuraminidase activity. In the presence of HRP, H2O2 reacts with a 1:1 stiochiometry with Amplex Red reagent to generate the red-fluorescent oxidation product, resorufin.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Citations & References (10)

Citations & References
Abstract
Filifactor alocis has virulence attributes that can enhance its persistence under oxidative stress conditions and mediate invasion of epithelial cells by porphyromonas gingivalis.
Authors:Aruni AW, Roy F, Fletcher HM,
Journal:Infect Immun
PubMed ID:21825062
'Filifactor alocis, a Gram-positive anaerobic rod, is one of the most abundant bacteria identified in the periodontal pockets of periodontitis patients. There is a gap in our understanding of its pathogenicity and ability to interact with other periodontal pathogens. To evaluate the virulence potential of F. alocis and its ability ... More
VimA-dependent modulation of acetyl coenzyme A levels and lipid A biosynthesis can alter virulence in Porphyromonas gingivalis.
Authors:Aruni AW, Lee J, Osbourne D, Dou Y, Roy F, Muthiah A, Boskovic DS, Fletcher HM,
Journal:Infect Immun
PubMed ID:22144476
'The Porphyromonas gingivalis VimA protein has multifunctional properties that can modulate several of its major virulence factors. To further characterize VimA, P. gingivalis FLL406 carrying an additional vimA gene and a vimA-defective mutant in a different P. gingivalis genetic background were evaluated. The vimA-defective mutant (FLL451) in the P. gingivalis ... More
Preterm human milk contains a large pool of latent TGF-ß, which can be activated by exogenous neuraminidase.
Authors:Namachivayam K, Blanco CL, Frost BL, Reeves AA, Jagadeeswaran R, MohanKumar K, Safarulla A, Mandal P, Garzon SA, Raj JU, Maheshwari A,
Journal:Am J Physiol Gastrointest Liver Physiol
PubMed ID:23558011
'Human milk contains substantial amounts of transforming growth factor (TGF)-ß, particularly the isoform TGF-ß2. We previously showed in preclinical models that enterally administered TGF-ß2 can protect against necrotizing enterocolitis (NEC), an inflammatory bowel necrosis of premature infants. In this study we hypothesized that premature infants remain at higher risk of ... More
Resistance of influenza viruses to neuraminidase inhibitors--a review.
Authors:McKimm-Breschkin JL
Journal:Antiviral Res
PubMed ID:10930642
Neuraminidase inhibition and viral chemotherapy.
Authors:Haskell TH, Peterson FE, Watson D, Plessas NR, Culbertson T
Journal:J Med Chem
PubMed ID:4318072
10 total citations

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